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GENIE' SINGLE CEILING AND DOUBLE CEILING

Page Type
Cleared 510(K)
510(k) Number
K963682
510(k) Type
Traditional
Applicant
BURTON MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1996
Days to Decision
71 days
Submission Type
Statement

GENIE' SINGLE CEILING AND DOUBLE CEILING

Page Type
Cleared 510(K)
510(k) Number
K963682
510(k) Type
Traditional
Applicant
BURTON MEDICAL PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1996
Days to Decision
71 days
Submission Type
Statement